Galantamine

Product NDC
72162-2566
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Galantamine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090957
Marketing category
ANDA
Substance
GALANTAMINE HYDROBROMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2566-660 TABLET, FILM COATED in 1 BOTTLE (72162-2566-6) 2025-11-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GalantamineBryant Ranch Prepack2025-11-04HUMAN PRESCRIPTION DRUG LABEL100